...
首页> 外文期刊>Journal of Applied Polymer Science >Chitosan-graft-acrylamide polyelectrolytes: Synthesis, flocculation, and modeling
【24h】

Chitosan-graft-acrylamide polyelectrolytes: Synthesis, flocculation, and modeling

机译:壳聚糖接枝丙烯酰胺聚电解质:合成,絮凝和建模

获取原文
获取原文并翻译 | 示例

摘要

A series of chitosans have been grafted with quaternary ammonium cationic monomers, as well as acrylamide using Ce(IV) to induce macroradical formation on the polysaccharide backbone. The materials, which have long chain branches per molecule between 0.3 and 5.5, are shown to provide very high specific flocculation efficiency, at the very least equal to the entirely synthetic materials which have been previously documented in the literature. A charge ratio, determined from the polymer concentration at which flocculation takes place, the charge density of the polymer, and the surface charge of the suspended matter are proposed as metrics to evaluate the occurrence of charge neutralization and bridging or charge patch flocculation mechanism. Furthermore, a window of application (WA) for flocculants, which characterizes the region of concentration wherein the polyelectrolyte can remove 99% of the supernatant turbidity, has been defined. It was shown to depend on the square root of the ionic strength and varies inversely with the Debye length, providing a fundamental basis for the concept of the WA. A mathematical expression is presented which links the WA with the salt concentration and the number of branches of the grafted polymer. Grafted chitosans have been shown to be more robust than polyacrylamides in testing against model kaolin suspensions. (c) 2006 Wiley Periodicals, Inc.
机译:使用Ce(IV)将一系列壳聚糖与季铵阳离子单体以及丙烯酰胺接枝,以诱导多糖主链上形成大自由基。具有每分子长链支链在0.3和5.5之间的材料显示出提供非常高的比絮凝效率,至少与先前文献中记载的完全合成的材料相等。提出了由发生絮凝的聚合物浓度,聚合物的电荷密度和悬浮物的表面电荷确定的电荷比,作为评估电荷中和和桥接或电荷斑块絮凝机理的度量。此外,已经定义了絮凝剂的应用窗口(WA),该窗口表征了聚电解质可以去除99%的上清液浊度的浓度区域。它显示出取决于离子强度的平方根,并且与德拜长度成反比,这为WA的概念提供了基础。提出了将WA与盐浓度和接枝聚合物的支链数量联系起来的数学表达式。在针对模型高岭土悬浮液的测试中,嫁接的壳聚糖已被证明比聚丙烯酰胺更坚固。 (c)2006年Wiley Periodicals,Inc.

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号